Anodyne

IC-26, WIN 1161-3
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
[]
Methiodone hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
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345.5 g/mol [1]
3.8 [1]
Structural Identifiers
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C20H27NO2[1]
4-ethylsulfonyl-N,N-dimethyl-4,4-diphenylbutan-2-amine [1]
CCS(=O)(=O)C(CC(C)N(C)C)(C1=CC=CC=C1)C2=CC=CC=C2 [1]
InChI=1S/C20H27NO2S/c1-5-24(22,23)20(16-17(2)21(3)4,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6-15,17H,5,16H2,1-4H3 [1]
InChIKeyNLPGJSPLDNDKKZ-UHFFFAOYSA-N [1]

Methiodone

Methiodone (also known as IC-26, Propylamine, 3-(ethylsulfonyl)-N,N,1-trimethyl-3,3-diphenyl-, γ-(Ethylsulfonyl)-N,N,α-trimethyl-γ-phenylbenzenepropanamine, Benzenepropanamine, γ-(ethylsulfonyl)-N,N,α-trimethyl-γ-phenyl-, γ-(Ethylsulfonyl)-n,n,α-trimethyl-γ-phenylbenzenepropanamine, Benzenepropanamine, γ-(ethylsulfonyl)-n,n,α-trimethyl-γ-phenyl-, RefChem:147585, WIN 1161-3 or 4-(ethanesulfonyl)-N,N-dimethyl-4,4-diphenylbutan-2-amine) is a opioid substance of the phenylpropylamine class.

Chemistry

Salts []

Methiodone is typically found in the form of its hydrochloride salt.

 []

Methiodone is a racemic mixture of the

Stereoisomers
(S)-MethiodoneGenerated by the Chemistry Development Kit (http://github.com/cdk)
(R)-MethiodoneGenerated by the Chemistry Development Kit (http://github.com/cdk)

Subjective effects []

Anodyne Usernotes
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magnus / Methiodone -

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 113832, Methiodone. Accessed September 1, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/113832

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Methiodone. UNII: ZSY3T8J4AQ. Global Substance Registration System. Accessed September 1, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/ZSY3T8J4AQ